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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzonitrile, 5-fluoro-2-hydroxy-

N#Cc1cc(F)ccc1O Request for Quotation
Chemical Name: Benzonitrile, 5-fluoro-2-hydroxy-
CAS Number: 91407-41-9
Product Number: AG006N7X(AGN-PC-00K354)
Synonyms:
MDL No: MFCD11846513
Molecular Formula: C7H4FNO
Molecular Weight: 137.1112

Identification/Properties

Properties
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
137.113g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
137.028g/mol
Monoisotopic Mass:
137.028g/mol
Topological Polar Surface Area:
44A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
162
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoro-2-hydroxybenzonitrile, also known as $name$, serves as a versatile building block in chemical synthesis due to its unique chemical properties. This compound is commonly utilized as a key intermediate in the pharmaceutical industry, playing a crucial role in the synthesis of various biologically active compounds.In organic synthesis, $name$ can undergo selective functional group transformations, such as nucleophilic substitution reactions, to introduce desired chemical moieties into the molecular structure. This makes it a valuable precursor for the preparation of pharmaceuticals, agrochemicals, and other fine chemicals.Furthermore, $name$ can participate in cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds, enabling the construction of complex molecular scaffolds. Its compatibility with a wide range of synthetic methodologies makes it a valuable tool for organic chemists engaged in drug discovery and development.Overall, the application of 5-Fluoro-2-hydroxybenzonitrile in chemical synthesis facilitates the efficient and strategic assembly of diverse molecular architectures, contributing to the advancement of medicinal chemistry and chemical research.